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{"Adverse Reaction Reports": 6, "Company": "PFIZER\\BIONTECH", "Deaths": 0, "Disabilities": 0, "Hospitalizations": 0, "Life-Threatening Illnesses": 0, "batchcode": "GE 3043", "histogram": {"Altered state of consciousness": 1, "Arthralgia": 2, "Asthenia": 1, "Atrial tachycardia": 1, "Balance disorder": 1, "Cognitive disorder": 1, "Contusion": 1, "Decreased appetite": 1, "Dizziness": 2, "Dysphagia": 1, "Ear pain": 1, "Fatigue": 2, "Gait disturbance": 1, "Glossodynia": 1, "Headache": 2, "Immunisation": 1, "Influenza like illness": 1, "Interchange of vaccine products": 1, "Kidney infection": 1, "Lethargy": 1, "Lymphadenopathy": 1, "Memory impairment": 1, "Metamorphopsia": 1, "Mobility decreased": 1, "Myoclonic epilepsy": 1, "Nausea": 1, "Off label use": 1, "Oropharyngeal pain": 1, "Pain in extremity": 3, "Partial seizures": 1, "Peripheral swelling": 1, "Pharyngeal swelling": 1, "Pyrexia": 2, "SARS-CoV-2 test": 5, "Sensory loss": 1, "Sinus pain": 1, "Swollen tongue": 1, "Tinnitus": 1, "Wrong product administered": 1}} |